Coordinator, Regulatory Operations

at  Cencora

Oakville, ON, Canada -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate01 Feb, 2025USD 47300 Annual03 Nov, 20243 year(s) or aboveClient Confidentiality,Regulatory Affairs,Project Management Skills,Regulatory Operations,Completion,Software,Timelines,Life Sciences,Electronic Submissions,Nees,Communication Skills,Microsoft Word,Time Management,Working Experience,Adobe AcrobatNoNo
Add to Wishlist Apply All Jobs
Required Visa Status:
CitizenGC
US CitizenStudent Visa
H1BCPT
OPTH4 Spouse of H1B
GC Green Card
Employment Type:
Full TimePart Time
PermanentIndependent - 1099
Contract – W2C2H Independent
C2H W2Contract – Corp 2 Corp
Contract to Hire – Corp 2 Corp

Description:

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today!

EXPERIENCE AND EDUCATIONAL REQUIREMENTS:

  • B.Sc in Life Sciences or typically 3-5 years of daily working experience in Regulatory Operations.

MINIMUM SKILLS, KNOWLEDGE AND ABILITY REQUIREMENTS:

  • Excellent written and verbal communication skills.
  • Excellent computer skills previous experience with Microsoft Word and Adobe Acrobat is an asset.
  • Some previous experience with Excel and Power Point is an asset.
  • Experience with Non-eCTD electronic Submissions (NeeS) and eCTD software an asset.
  • Knowledge of industry guidance’s (Regulatory Operations related and some Regulatory Affairs related), would be an asset to have.
  • Ability to multitask with the aim of balancing several projects at once.
  • Must have a good understanding of client confidentiality and the importance not to cross project information with one another.
  • Results oriented with proven time management, organization and prioritizing skills.
  • Must have an acute ability for attention to detail.
  • Ability to work well individually and as a team.
  • Has a positive attitude and works for the greater good of our clients, the team and the company.
  • Is responsible for company supplied hardware and software; contacting Innomar IT when needed for assistance.
  • Ability to obtain individual and department goals.
  • Excellent project management skills – expected to see all projects through to completion. Expected to have the ability to coordinate with other team members in order to complete all projects on time and advise manager if timelines will not be met and/or help is required. Able to keep accurate, up-to-date records as per company/department guidelines.
  • Ability to consistently meet extremely tight deadlines.
  • Excellent conflict resolution capabilities and ability to spearhead issues (professionally) and successfully solve as they arise.

EQUAL EMPLOYMENT OPPORTUNITY

Cencora is committed to providing equal employment opportunity without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, age, disability, veteran status or membership in any other class protected by federal, state or local law.
The company’s continued success depends on the full and effective utilization of qualified individuals. Therefore, harassment is prohibited and all matters related to recruiting, training, compensation, benefits, promotions and transfers comply with equal opportunity principles and are non-discriminatory.
Cencora is committed to providing reasonable accommodations to individuals with disabilities during the employment process which are consistent with legal requirements. If you wish to request an accommodation while seeking employment, please call 888.692.2272 or email hrsc@cencora.com. We will make accommodation determinations on a request-by-request basis. Messages and emails regarding anything other than accommodations requests will not be returned

Responsibilities:

  • Build and maintain a positive and productive liaison with internal and external contacts, including interfacing with potential clients.
  • Use various internet document transfer sites to download client files and upload files ready to be sent back to our clients.
  • Use, manage and maintain submission files on the company shared drive and submissions drive as per company standard.
  • Create and format e-compliant documents as per clients’ needs using Microsoft Word, Adobe Acrobat (and associated plug-ins), Excel, Power Point.
  • Create eCTD submissions using the eCTD submissions builder, validation software and electronic submissions viewer.
  • Create NeeS, and paper submissions as needed.
  • Quality checking smaller, basic daily submissions until experience is gained to progress further.
  • Trouble shoot issues on a document level independently. Troubleshooting on a submission level with the help of your manager.
  • Send eCTD submissions via the ESG and CESG gateway.
  • Burn CDs/DVDs, create appropriate labelling.
  • Create courier waybills, pack and ship submission materials as needed.
  • Enter time into Paymo, or company chosen database, on a daily basis.
  • Attend and contribute to weekly department meetings.
  • Obtain and maintain professional regulatory and documentary knowledge in order to provide effective consulting advice.
  • The Coordinator may be asked to complete additional and other department services as required.


REQUIREMENT SUMMARY

Min:3.0Max:5.0 year(s)

Human Resources/HR

Pharma / Biotech / Healthcare / Medical / R&D

HR

BSc

Regulatory operations

Proficient

1

Oakville, ON, Canada